1973
DOI: 10.1159/000149421
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Indirect Hemagglutination for Diagnosis of Crimean Hemorrhagic Fever

Abstract: An indirect hemagglutination (IHA) test with Congo and Crimean hemorrhagic fever (CHF) viruses employing sheep erythrocytes sensitized with immune γ-globulin was developed. The titer of the IHA test with sucrose acetone antigens of the virus reached 1:16,000–1:32,000; the reaction was specifically inhibited in the presence of immune sera and sera of CHF-convalescent patients. High sensitivity and specificity of the reaction recommend it for the serodiagnostics of CHF.

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Cited by 8 publications
(6 citation statements)
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“…Anti-CCHFV antibodies, detected by agar-gel diffusion precipitation (AGDP) performed 5–20 dpi in samples from the 6-month-old calves, were seen at 13 and 17 dpi in the SC-infected and the IM-infected calf, respectively; antibodies were detected by CF only in the IM-infected animal (17 dpi). Additionally, antibodies were investigated in the SC/ID inoculated 2-month-old calves using the indirect hemagglutination inhibition test 5–35 dpi (47); antibody titers of 1:10 were detected in 1 calf on days 9, 14, and 20 after infection, increasing to 1:80 at 35 dpi. Smirnova (1979) inoculated calves with a variety of strains of CCHFV (48).…”
Section: Experimental Infection In Livestockmentioning
confidence: 99%
“…Anti-CCHFV antibodies, detected by agar-gel diffusion precipitation (AGDP) performed 5–20 dpi in samples from the 6-month-old calves, were seen at 13 and 17 dpi in the SC-infected and the IM-infected calf, respectively; antibodies were detected by CF only in the IM-infected animal (17 dpi). Additionally, antibodies were investigated in the SC/ID inoculated 2-month-old calves using the indirect hemagglutination inhibition test 5–35 dpi (47); antibody titers of 1:10 were detected in 1 calf on days 9, 14, and 20 after infection, increasing to 1:80 at 35 dpi. Smirnova (1979) inoculated calves with a variety of strains of CCHFV (48).…”
Section: Experimental Infection In Livestockmentioning
confidence: 99%
“…Seroepidemiological studies comprise the majority of this research, elucidating reservoir species and virus circulation. CCHFV serosurveillance has relied on a variety of techniques, including virus neutralization assays [ 9 , 10 ], reverse passive hemagglutination inhibition (RPHI) assays [ 11 13 ], immunodiffusion assays such as agar gel diffusion precipitation (AGDP) [ 14 , 15 ], complement fixation (CF) assays [ 9 , 16 – 18 ], indirect immunofluorescence assays (IFA) [ 19 23 ], indirect or sandwich enzyme-linked immunoassays (ELISA) [ 23 27 ], and competitive ELISA (CELISA) [ 28 ].…”
Section: Introductionmentioning
confidence: 99%
“…Virus antigen can be detected in ticks and in tissues of infected mice and humans, by passive haemagglutination or enzyme-linked immunoassay (ELISA), but positive results were obtained in only about half of the patients from whom sera were tested during the first 2 weeks of illness, with greatest success being attained in severe and fatal infections with the most intense viraemias [4,[6][7][8][9][10]. Serological tests formerly used for the detection of antibody to the virus, such as complement fixation, haemagglutination-inhibition and reversed passive haemagglutinationinhibition, lacked sensitivity and reproducibility, but indirect immunofluorescence (IF) detects IgG and IgM antibody responses by days 7-9 of illness in all survivors of the infection [11][12][13][14]. Specific IgG and IgM responses can also be detected by ELISA, but tests have as yet been applied to very few patients [9,11].…”
Section: Introductionmentioning
confidence: 99%